NDC 68151-4982 Abilify
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-4982 - Abilify
Product Characteristics
Product Packages
NDC Code 68151-4982-1
Package Description: 1 TABLET in 1 PACKAGE
Product Details
What is NDC 68151-4982?
What are the uses for Abilify?
Which are Abilify UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARIPIPRAZOLE (UNII: 82VFR53I78)
- ARIPIPRAZOLE (UNII: 82VFR53I78) (Active Moiety)
Which are Abilify Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- STARCH, CORN (UNII: O8232NY3SJ)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Abilify?
- RxCUI: 402131 - ARIPiprazole 5 MG Oral Tablet
- RxCUI: 402131 - aripiprazole 5 MG Oral Tablet
- RxCUI: 404602 - ABILIFY 5 MG Oral Tablet
- RxCUI: 404602 - aripiprazole 5 MG Oral Tablet [Abilify]
- RxCUI: 404602 - Abilify 5 MG Oral Tablet
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".